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rs6133

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs6133(G;T)
Make rs6133(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position169596108
GeneSELP
is asnp
is mentioned by
dbSNPrs6133
ebirs6133
HLIrs6133
Exacrs6133
Varsomers6133
Maprs6133
PheGenIrs6133
hapmaprs6133
1000 genomesrs6133
hgdprs6133
ensemblrs6133
gopubmedrs6133
geneviewrs6133
scholarrs6133
googlers6133
pharmgkbrs6133
gwascentralrs6133
openSNPrs6133
23andMers6133
23andMe allrs6133
SNP Nexus

SNPshotrs6133
SNPdbers6133
MSV3drs6133
GWAS Ctlgrs6133
GMAF0.1993
Max Magnitude0
? (G;G) (G;T) (T;T) 28
OMIM173610
DescATOPY, SUSCEPTIBILITY TO
Variant0002
Relatedalso
[PMID 19404301OA-icon.png] Variation in the upstream region of P-Selectin (SELP) is a risk factor for SLE


[PMID 19240957] Candidate gene analysis of selectin cluster in patients with multiple sclerosis


ClinVar
Risk rs6133(C,T;C,T)
Alt rs6133(C,T;C,T)
Reference rs6133(G;G)
Significance Other
Disease Atopy
Variation info
Gene SELP
CLNDBN Atopy, susceptibility to
Reversed 1
HGVS NC_000001.10:g.169565346C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000014483.2,



[PMID 15726497OA-icon.png] Gene-environment interaction effects on the development of immune responses in the 1st year of life.


[PMID 16820586OA-icon.png] Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery.


[PMID 19131662OA-icon.png] A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.


[PMID 19263529OA-icon.png] Genetic risk factors in recurrent venous thromboembolism: A multilocus, population-based, prospective approach.


[PMID 19330901OA-icon.png] Association of 77 polymorphisms in 52 candidate genes with blood pressure progression and incident hypertension: the Women's Genome Health Study.


[PMID 19559392OA-icon.png] A candidate gene association study of 77 polymorphisms in migraine.


GET Evidence
SELP-V640L
aa_change Val640Leu
aa_change_short V640L
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.26966
summary



[PMID 24504449] SELP genetic polymorphisms may contribute to the pathogenesis of coronary heart disease and myocardial infarction: a meta-analysis